Canonical Allele Identifier: CA10505462
Community Standard Title: NM_001079872.2(CUL4B):c.2023A>G (p.Met675Val)
Gene: CUL4B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.120536950T>C , CM000685.2:g.120536950T>C GRCh38
NC_000023.10:g.119670805T>C , CM000685.1:g.119670805T>C GRCh37
NC_000023.9:g.119554833T>C NCBI36
NG_009388.1:g.43880A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001079872.2:c.2023A>G MANE Select NP_001073341.1:p.Met675Val
ENST00000371322.11:c.2023A>G MANE Select ENSP00000360373.5:p.Met675Val
NM_001079872.1:c.2023A>G NP_001073341.1:p.Met675Val
NM_001330624.1:c.2038A>G NP_001317553.1:p.Met680Val
NM_001330624.2:c.2038A>G NP_001317553.1:p.Met680Val
NM_001369145.1:c.1489A>G NP_001356074.1:p.Met497Val
NM_003588.3:c.2077A>G NP_003579.3:p.Met693Val
NM_003588.4:c.2077A>G NP_003579.3:p.Met693Val
ENST00000336592.10:c.2038A>G ENSP00000338919.6:p.Met680Val
ENST00000336592.11:c.2038A>G ENSP00000338919.6:p.Met680Val
ENST00000371322.9:c.2023A>G ENSP00000360373.5:p.Met675Val
ENST00000371323.3:c.1489A>G ENSP00000360374.3:p.Met497Val
ENST00000404115.7:c.2077A>G ENSP00000384109.3:p.Met693Val
ENST00000404115.8:c.2023A>G ENSP00000384109.4:p.Met675Val
ENST00000497616.1:n.509A>G
ENST00000497616.2:n.364A>G
ENST00000673919.1:c.*1470A>G ENSP00000500994.1:n.*1470A>G
ENST00000674073.2:c.1467A>G
ENST00000674137.11:c.2029A>G ENSP00000501019.6:p.Met677Val
ENST00000679405.1:c.*1232A>G ENSP00000504985.1:n.*1232A>G
ENST00000679432.1:c.2128A>G
ENST00000679844.1:c.1362A>G
ENST00000679927.1:c.1678A>G ENSP00000505603.1:p.Met560Val
ENST00000679965.1:n.603A>G
ENST00000680165.1:n.2799A>G
ENST00000680324.1:n.3431A>G
ENST00000680457.1:n.1451A>G
ENST00000680474.1:c.1467A>G
ENST00000680577.1:n.2634A>G
ENST00000680673.1:c.2077A>G ENSP00000505084.1:p.Met693Val
ENST00000680918.1:c.1304A>G
ENST00000681080.1:c.1513A>G
ENST00000681090.1:c.1930A>G ENSP00000506288.1:p.Met644Val
ENST00000681189.1:c.1529A>G
ENST00000681206.1:c.2137A>G ENSP00000505480.1:p.Met713Val
ENST00000681253.1:c.2077A>G ENSP00000506259.1:p.Met693Val
ENST00000681263.1:n.867A>G
ENST00000681333.1:c.*2916A>G ENSP00000505739.1:n.*2916A>G
ENST00000681652.1:c.2077A>G ENSP00000505176.1:p.Met693Val
ENST00000681864.1:n.4611A>G
ENST00000681869.1:c.1467A>G
ENST00000681908.1:c.1643A>G
XM_005262481.1:c.2083A>G XP_005262538.1:p.Met695Val
XM_006724784.1:c.2044A>G XP_006724847.1:p.Met682Val
XM_006724785.1:c.2038A>G XP_006724848.1:p.Met680Val
XM_011531399.1:c.1495A>G XP_011529701.1:p.Met499Val
XM_011531399.2:c.1495A>G XP_011529701.1:p.Met499Val
XM_011531400.1:c.1489A>G XP_011529702.1:p.Met497Val
XM_011531400.2:c.1489A>G XP_011529702.1:p.Met497Val
XM_011531401.1:c.1441A>G XP_011529703.1:p.Met481Val